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Atlastin GTPases are required for Golgi apparatus and ER morphogenesis
The hereditary spastic paraplegias (SPG1-33) comprise a cluster of inherited neurological disorders characterized principally by lower extremity spasticity and weakness due to a length-dependent, retrograde axonopathy of corticospinal motor neurons. Mutations in the gene encoding the large oligomeri...
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| 主要な著者: | , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2008
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2902292/ https://ncbi.nlm.nih.gov/pubmed/18270207 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn046 |
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